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Escitalopram Oxalate
Escitalopram Oxalate - 51672-1348-1 - (Escitalopram Oxalate)
Drug Information of Escitalopram Oxalate
| Product NDC: | 51672-1348 |
| Proprietary Name: | Escitalopram Oxalate |
| Non Proprietary Name: | Escitalopram Oxalate |
| Active Ingredient(s): | 5 mg/5mL & nbsp; Escitalopram Oxalate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Escitalopram Oxalate
| Product NDC: | 51672-1348 |
| Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079121 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120503 |
Package Information of Escitalopram Oxalate
| Package NDC: | 51672-1348-1 |
| Package Description: | 1 BOTTLE in 1 CARTON (51672-1348-1) > 240 mL in 1 BOTTLE |
NDC Information of Escitalopram Oxalate
| NDC Code | 51672-1348-1 |
| Proprietary Name | Escitalopram Oxalate |
| Package Description | 1 BOTTLE in 1 CARTON (51672-1348-1) > 240 mL in 1 BOTTLE |
| Product NDC | 51672-1348 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Escitalopram Oxalate |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20120503 |
| Marketing Category Name | ANDA |
| Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
| Substance Name | ESCITALOPRAM OXALATE |
| Strength Number | 5 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
